Primary Device ID | 05415334001435 |
NIH Device Record Key | 26463d3a-2d2a-4339-91b3-a33e883a1218 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Nio 3MP |
Version Model Number | E-3620 |
Catalog Number | K9300248B |
Company DUNS | 371618773 |
Company Name | Barco NV |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com | |
Phone | +1(866)302-7939 |
service.medical.usa@barco.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05415334001435 [Primary] |
LLZ | System, image processing, radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-12-20 |
Device Publish Date | 2016-08-19 |
05415334001442 | E-3620 MA LORAD G |
05415334001435 | E-3620 MA |